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352535-68-3

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352535-68-3 Usage

General Description

(S)-(-)N-Carbomethoxy-alpha,alpha-diphenyl-2-pyrrolidinemethanol is a chemical compound that is 98% pure. It is an enantiomer of N-carbomethoxy-alpha,alpha-diphenyl-2-pyrrolidinemethanol, meaning it has a specific three-dimensional arrangement of its atoms. (S)-(-)N-CARBOMETHOXY-ALPHA,ALPHA-DIPHENYL -2-PYRROLIDINEMETHANOL,98% is commonly used in organic synthesis as a chiral auxiliary, which means it can help to control the stereochemistry of a reaction. It can also be used in the preparation of pharmaceutical compounds and other organic molecules where stereochemistry is important. The high level of purity of this chemical makes it particularly useful for these applications.

Check Digit Verification of cas no

The CAS Registry Mumber 352535-68-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,5,3 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 352535-68:
(8*3)+(7*5)+(6*2)+(5*5)+(4*3)+(3*5)+(2*6)+(1*8)=143
143 % 10 = 3
So 352535-68-3 is a valid CAS Registry Number.

352535-68-3 Well-known Company Product Price

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  • Aldrich

  • (554448)  Methyl(2S)-(−)-2-(hydroxydiphenylmethyl)-1-pyrrolidinecarboxylate  98%

  • 352535-68-3

  • 554448-500MG

  • 1,028.43CNY

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352535-68-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (2S)-2-[hydroxy(diphenyl)methyl]pyrrolidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:352535-68-3 SDS

352535-68-3Relevant articles and documents

Lanthanide Lewis acid-mediated enantioselective conjugate radical additions

Sibi, Mukund P.,Manyem, Shankar

, p. 2929 - 2932 (2007/10/03)

(figure presented) Lanthanide triflates along with proline-derived ligands have been found to be efficient catalysts for enantioselective conjugate addition of nucleophilic radicals to enoates. N-Acyl oxazolidinones, when used as achiral additives, gave meaningful enhancements in the ees for the product.

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